chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124502704045027041CT35GENIChomozygous115338992
124502865845028659GA32GENIChomozygous115338998
124502912245029123TG31GENICpossibly homozygous115391998
124502915345029154CT36GENIChomozygous115392000
124502952545029526CA15GENIChomozygous115339002
124502963745029638AG29GENIChomozygous115339004
124502966745029668TC31GENIChomozygous115339006
124502986045029861CA41GENIChomozygous115392002
124503004845030049TC23GENIChomozygous115339008
124503070745030708TC28GENIChomozygous115339010
124503108545031086GA22GENIChomozygous115339012